3-(ETHYLCARBAMOYL)-4-FLUOROBENZENEBORONIC ACID
98%
- Product Code: 90025
CAS:
874219-20-2
| Molecular Weight: | 210.9979 g./mol | Molecular Formula: | C₉H₁₁BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08235039 | |
| Melting Point: | 260-262 °C | Boiling Point: | |
| Density: | 1.27 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its ethylcarbamoyl and fluoro substituents enhance its reactivity and selectivity in specific chemical transformations, contributing to its use in the development of targeted drug molecules and bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,750.00 |
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| 1.000 | 10-20 days | ฿17,820.00 |
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3-(ETHYLCARBAMOYL)-4-FLUOROBENZENEBORONIC ACID
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its ethylcarbamoyl and fluoro substituents enhance its reactivity and selectivity in specific chemical transformations, contributing to its use in the development of targeted drug molecules and bioactive compounds.
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